494798-06-0

Upstream product

• 374073-49-1 2-allyl-3-ethoxy-4-methoxybenzaldehyde 
• 621-59-0 isovanillin 
• 18075-41-7 2-allyl-3-hydroxy-4-methoxybenzaldehyde 
• 18075-40-6 O-allylisovanillin 

Downstream Products

• 881199-44-6 2-allyl-1-[(2-allyl-3-ethoxy-4-methoxybenzyl)oxy]-3-isopropoxy-4-methoxybenzene 
• 881199-42-4 2-allyl-1-[(2-allyl-3-ethoxy-4-methoxybenzyl)oxy]-3-ethoxy-4-methoxybenzene 
• 881199-39-9 2-allyl-1-[(2-allyl-3-ethoxy-4-methoxybenzyl)oxy]-3,4-dimethoxybenzene 
• 494798-13-9 2-allyl-1-allyloxymethyl-3-ethoxy-4-methoxybenzene 

Relevant academic research and scientific papers

Synthesis of dibenzo-fused 10-membered cyclic ethers from isovanillin Via ring-closing metathesis

A synthesis of substituted dibenzo-fused 10-membered cyclic ethers is described. 2-Allylbenzyl alcohols and 2-allylphenols derived from isovanillin were coupled by the Mitsunobu reaction to construct intramolecular dienes with ether linkage. The resulting

A synthesis of substituted 3,6-dihydro-1H-benzo[c]oxocines via Claisen rearrangement and ring-closing metathesis

Started from isovanillin, based on Claisen rearrangement and ring-closing metathesis (RCM) reaction, a series of substituted 3,6-dihydro-1H-benzo[c]oxocines were synthesized in moderate yields.